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Details

Stereochemistry RACEMIC
Molecular Formula C5H9NO2S
Molecular Weight 147.195
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Methyl 1,3-thiazolidine-4-carboxylate

SMILES

COC(=O)C1CSCN1

InChI

InChIKey=NHBNAVLHRAPNKY-UHFFFAOYSA-N
InChI=1S/C5H9NO2S/c1-8-5(7)4-2-9-3-6-4/h4,6H,2-3H2,1H3

HIDE SMILES / InChI
Molecular Formula C5H9NO2S
Molecular Weight 147.195
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Unknown
139594
Substance Class Chemical
Created
by admin
on Sat Dec 16 10:32:23 GMT 2023
Edited
by admin
on Sat Dec 16 10:32:23 GMT 2023
Record UNII
8VLB09VT95
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
Methyl 1,3-thiazolidine-4-carboxylate
Systematic Name English
METHYL 4-THIAZOLIDINECARBOXYLATE
Systematic Name English
4-CARBOMETHOXYTHIAZOLINE
Systematic Name English
4-(METHOXYCARBONYL)THIAZOLIDINE
Systematic Name English
4-THIAZOLIDINECARBOXYLIC ACID, METHYL ESTER
Common Name English
4-methoxycarbonylthiazolidinium [WHO-DD]
Common Name English
METHYL THIAZOLIDINE-4-CARBOXYLATE
Systematic Name English
Code System Code Type Description
ECHA (EC/EINECS)
262-361-2
Created by admin on Sat Dec 16 10:32:23 GMT 2023 , Edited by admin on Sat Dec 16 10:32:23 GMT 2023
PRIMARY
EVMPD
SUB12688MIG
Created by admin on Sat Dec 16 10:32:23 GMT 2023 , Edited by admin on Sat Dec 16 10:32:23 GMT 2023
ALTERNATIVE
CAS
60667-24-5
Created by admin on Sat Dec 16 10:32:23 GMT 2023 , Edited by admin on Sat Dec 16 10:32:23 GMT 2023
PRIMARY
FDA UNII
8VLB09VT95
Created by admin on Sat Dec 16 10:32:23 GMT 2023 , Edited by admin on Sat Dec 16 10:32:23 GMT 2023
PRIMARY
PUBCHEM
93329
Created by admin on Sat Dec 16 10:32:23 GMT 2023 , Edited by admin on Sat Dec 16 10:32:23 GMT 2023
PRIMARY
EVMPD
SUB12689MIG
Created by admin on Sat Dec 16 10:32:23 GMT 2023 , Edited by admin on Sat Dec 16 10:32:23 GMT 2023
PRIMARY
Related Record Type Details
Structure of methyl (4S)-1,3-thiazolidine-4-carboxylate
ENANTIOMER -> RACEMATE
Structure of methyl (4R)-1,3-thiazolidine-4-carboxylate
ENANTIOMER -> RACEMATE
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